FDA UDI In Commercial Distribution 🇺🇸 United States

J-PLASMA® PRECISE™

DI: 00607151011987 · Model: BVX-500BF · BOVIE MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
J-PLASMA® PRECISE™
Primary DI
00607151011987
Version / Model
BVX-500BF
Catalog Number
BVX-500BF
Company Name
BOVIE MEDICAL CORPORATION
Labeler DUNS
079940465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-03
Public Version
4
Public Version Date
2019-02-21
Public Version Status
Update
Public Device Record Key
f0d256cb-a907-45d2-a542-e0d5026dd0a4

Device Description

J-PLASMA® PRECISE™ FLEX, 500mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Primary 00607151011987
Package 10607151011984

Premarket Submissions

Submission Number Supplement Number
K170777 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius